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Replication Stress-Induced Genome Instability: The Dark Side of Replication Maintenance by Homologous Recombination

Journal

JOURNAL OF MOLECULAR BIOLOGY
Volume 425, Issue 23, Pages 4733-4744

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jmb.2013.04.023

Keywords

homologous recombination; DNA replication; genome instability; genomic disorders

Funding

  1. Agence Nationale de la Recherche [ANR-Piribio09-44854, ANRJCJC10-120301]
  2. La Ligue Contre le Cancer (Comite Essonne)
  3. Medical Research Council [G1100074]
  4. Association for International Cancer Research grant [12-1118]
  5. MRC [G1100074] Funding Source: UKRI
  6. Medical Research Council [G1100074, G0801130B] Funding Source: researchfish
  7. Worldwide Cancer Research [12-1118] Funding Source: researchfish

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Homologous recombination (HR) is an evolutionary-conserved mechanism involved in a subtle balance between genome stability and diversity. HR is a faithful DNA repair pathway and has been largely characterized in the context of double-strand break (DSB) repair. Recently, multiple functions for the HR machinery have been identified at arrested forks. These are evident across different organisms and include replication fork-stabilization and fork-restart functions. Interestingly, a DSB appears not to be a prerequisite for HR-mediated replication maintenance. HR has the ability to rebuild a replisome at inactivated forks, but perhaps surprisingly, the resulting replisome is liable to intrastrand and interstrand switches leading to replication errors. Here, we review our current understanding of the replication maintenance function of HR. The error proneness of these pathways leads us to suggest that the origin of replication-associated genome instability should be re-evaluated. (C) 2013 Elsevier Ltd. All rights reserved.

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